De Novo Design of AC-P19M, a Novel Anticancer Peptide with Apoptotic Effects on Lung Cancer Cells and Anti-Angiogenic Activity.
Min Kyoung ShinBo-Young JangKyung-Bin BuSeung-Ho LeeDong-Hee HanJin Wook OhJung-Suk SungPublished in: International journal of molecular sciences (2022)
Despite the current developments in cancer therapeutics, efforts to excavate new anticancer agents continue rigorously due to obstacles, such as side effects and drug resistance. Anticancer peptides (ACPs) can be utilized to treat cancer because of their effectiveness on a variety of molecular targets, along with high selectivity and specificity for cancer cells. In the present study, a novel ACP was de novo designed using in silico methods, and its functionality and molecular mechanisms of action were explored. AC-P19M was discovered through functional prediction and sequence modification based on peptide sequences currently available in the database. The peptide exhibited anticancer activity against lung cancer cells, A549 and H460, by disrupting cellular membranes and inducing apoptosis while showing low toxicity towards normal and red blood cells. In addition, the peptide inhibited the migration and invasion of lung cancer cells and reversed epithelial-mesenchymal transition. Moreover, AC-P19M showed anti-angiogenic activity through the inhibition of vascular endothelial growth factor receptor 2 signaling. Our findings suggest that AC-P19M is a novel ACP that directly or indirectly targets cancer cells, demonstrating the potential development of an anticancer agent and providing insights into the discovery of functional substances based on an in silico approach.
Keyphrases
- vascular endothelial growth factor
- epithelial mesenchymal transition
- papillary thyroid
- red blood cell
- cell death
- small molecule
- squamous cell
- randomized controlled trial
- molecular docking
- transforming growth factor
- endothelial cells
- drinking water
- emergency department
- amino acid
- lymph node metastasis
- signaling pathway
- climate change
- cell cycle arrest
- single molecule
- childhood cancer
- electronic health record
- human health
- genetic diversity